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Characterization of Plasmodium falciparum adenylyl cyclase-? and its role in erythrocytic stage parasites.


ABSTRACT: The most severe form of human malaria is caused by the parasite Plasmodium falciparum. The second messenger cAMP has been shown to be important for the parasite's ability to infect the host's liver, but its role during parasite growth inside erythrocytes, the stage responsible for symptomatic malaria, is less clear. The P. falciparum genome encodes two adenylyl cyclases, the enzymes that synthesize cAMP, PfAC? and PfAC?. We now show that one of these, PfAC?, plays an important role during the erythrocytic stage of the P. falciparum life cycle. Biochemical characterization of PfAC? revealed a marked pH dependence, and sensitivity to a number of small molecule inhibitors. These inhibitors kill parasites growing inside red blood cells. One particular inhibitor is selective for PfAC? relative to its human ortholog, soluble adenylyl cyclase (sAC); thus, PfAC? represents a potential target for development of safe and effective antimalarial therapeutics.

SUBMITTER: Salazar E 

PROVIDER: S-EPMC3383692 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Characterization of Plasmodium falciparum adenylyl cyclase-β and its role in erythrocytic stage parasites.

Salazar Eric E   Bank Erin M EM   Ramsey Nicole N   Hess Kenneth C KC   Deitsch Kirk W KW   Levin Lonny R LR   Buck Jochen J  

PloS one 20120626 6


The most severe form of human malaria is caused by the parasite Plasmodium falciparum. The second messenger cAMP has been shown to be important for the parasite's ability to infect the host's liver, but its role during parasite growth inside erythrocytes, the stage responsible for symptomatic malaria, is less clear. The P. falciparum genome encodes two adenylyl cyclases, the enzymes that synthesize cAMP, PfACα and PfACβ. We now show that one of these, PfACβ, plays an important role during the er  ...[more]

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